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Structure of 344298-51-7
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Methyl 2-chloro-4-methoxynicotinate is a bench-stable, moisture-tolerant heterocyclic ester featuring a chlorine atom at the 2-position and a methoxy group at the 4-position of the pyridine ring. This electron-deficient scaffold integrates readily into synthetic sequences requiring directed functionalization, enabling efficient access to bioactive analogs through palladium-catalyzed cross-coupling and nucleophilic substitution reactions.
Methyl 2-chloro-4-methoxynicotinate serves as a versatile building block in medicinal chemistry and heterocyclic synthesis. Its ortho-chloro and meta-methoxy substituents enable selective functionalization, facilitating palladium-catalyzed cross-couplings and nucleophilic substitution reactions. The ester group supports further transformations including hydrolysis and derivatization. Bench-stable and readily purified by crystallization, it functions efficiently in the construction of bioactive scaffolds and API intermediates.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: